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Article

Maternal meiosis II nondisjunction in trisomy 21 is associated with maternal low socioeconomic status

1 Nov 2004

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Share to Down syndrome and intellectual disability research
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15545744
DOI: 10.1097/01.gim.0000144017.39690.4e

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Maternal meiosis II nondisjunction in trisomy 21 is associated with maternal low socioeconomic statusPMID 15545744Read ↗

A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21.Semantic proximity Read ↗

Nondisjunction in trisomy 21: Origin and mechanismsSemantic proximity Read ↗

New Insights into Human Nondisjunction of Chromosome 21 in OocytesSemantic proximity Read ↗

Nondisjunction in Trisomy 21: Origin and MechanismsSemantic proximity Read ↗

Risk factors for nondisjunction of trisomy 21Semantic proximity Read ↗

Telomere length is associated with types of chromosome 21 nondisjunction: a new insight into the maternal age effect on Down syndrome birthSemantic proximity Read ↗

The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphismsSemantic proximity Read ↗

Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome ProjectsSemantic proximity Read ↗

Trisomy 21 and Assisted Reproductive Technologies: A reviewSemantic proximity Read ↗

Understanding Etiology of Chromosome 21 Nondisjunction from Gene X Environment ModelsSemantic proximity Read ↗

Susceptible chiasmate configurations of chromosome 21 predispose to non–disjunction in both maternal meiosis I and meiosis IISemantic proximity Read ↗

The etiology of Down syndrome: Maternal MCM9 polymorphisms increase risk of reduced recombination and nondisjunction of chromosome 21 during meiosis I within oocyte.Semantic proximity Read ↗

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